Your browser doesn't support javascript.
loading
The role of efferocytosis-fueled macrophage metabolism in the resolution of inflammation.
Schilperoort, Maaike; Ngai, David; Sukka, Santosh R; Avrampou, Kleopatra; Shi, Hongxue; Tabas, Ira.
Afiliação
  • Schilperoort M; Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.
  • Ngai D; Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.
  • Sukka SR; Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.
  • Avrampou K; Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.
  • Shi H; Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.
  • Tabas I; Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.
Immunol Rev ; 319(1): 65-80, 2023 10.
Article em En | MEDLINE | ID: mdl-37158427
The phagocytosis of dying cells by macrophages, termed efferocytosis, is a tightly regulated process that involves the sensing, binding, engulfment, and digestion of apoptotic cells. Efferocytosis not only prevents tissue necrosis and inflammation caused by secondary necrosis of dying cells, but it also promotes pro-resolving signaling in macrophages, which is essential for tissue resolution and repair following injury or inflammation. An important factor that contributes to this pro-resolving reprogramming is the cargo that is released from apoptotic cells after their engulfment and phagolysosomal digestion by macrophages. The apoptotic cell cargo contains amino acids, nucleotides, fatty acids, and cholesterol that function as metabolites and signaling molecules to bring about this re-programming. Here, we review efferocytosis-induced changes in macrophage metabolism that mediate the pro-resolving functions of macrophages. We also discuss various strategies, challenges, and future perspectives related to drugging efferocytosis-fueled macrophage metabolism as strategy to dampen inflammation and promote resolution in chronic inflammatory diseases.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fagocitose / Apoptose Limite: Humans Idioma: En Revista: Immunol Rev Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fagocitose / Apoptose Limite: Humans Idioma: En Revista: Immunol Rev Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido